Canonical Allele Identifier: CA341877661

Gene: NOTCH2

Linked Data

• MyVariant Identifiers: chr1:g.120510091T>C (hg19) ; chr1:g.119967468T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119967468T>C , CM000663.2:g.119967468T>C	GRCh38
NC_000001.10:g.120510091T>C , CM000663.1:g.120510091T>C	GRCh37
NC_000001.9:g.120311614T>C	NCBI36
NG_008163.1:g.107186A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256646.7:c.1418A>G MANE Select	ENSP00000256646.2:p.Asp473Gly
ENST00000640021.1:c.638A>G	ENSP00000492223.1:n.638A>G
ENST00000256646.6:c.1418A>G	ENSP00000256646.2:p.Asp473Gly
ENST00000479412.2:n.1556A>G
ENST00000579475.7:c.1301A>G	ENSP00000477065.2:p.Asp434Gly
NM_001200001.1:c.1418A>G	NP_001186930.1:p.Asp473Gly
NM_024408.3:c.1418A>G	NP_077719.2:p.Asp473Gly
XM_005270901.2:c.1301A>G	XP_005270958.1:p.Asp434Gly
XM_011541519.1:c.1406A>G	XP_011539821.1:p.Asp469Gly
XM_011541520.1:c.1301A>G	XP_011539822.1:p.Asp434Gly
NM_024408.4:c.1418A>G MANE Select	NP_077719.2:p.Asp473Gly
NM_001200001.2:c.1418A>G	NP_001186930.1:p.Asp473Gly